Equisetin Targets Intracellular Staphylococcus aureus through a Host Acting Strategy |
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Authors: | Jiayao Tian Shang Chen Fei Liu Qian Zhu Jianzhong Shen Wenhan Lin Kui Zhu |
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Affiliation: | 1.National Center for Veterinary Drug Safety Evaluation, College of Veterinary Medicine, China Agricultural University, No. 2 Yuanmingyuan West Road, Beijing 100193, China;2.Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510642, China;3.State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, China |
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Abstract: | Mammalian cells act as reservoirs of internalized bacteria to circumvent extracellular antibacterial compounds, resulting in relapse and reinfection diseases. The intracellular persistence of Staphylococcus aureus renders most traditional antibiotics useless, due to their inadequate subcellular accumulation. To replenish our antibiotic arsenal, we found that a marine-derived compound, equisetin, efficiently eliminates intracellular S. aureus by potentiating the host autophagy and inducing mitochondrial-mediated ROS generation to clear the invading S. aureus. The remarkable anti-infection activity of equisetin was validated in a peritonitis-infected mouse model. The marine product equisetin utilizes a unique dual mechanism to modulate the host–pathogen interaction in the clearance of intracellular bacteria. Thus, equisetin is an inspiring host-acting candidate for overcoming intracellular pathogens. |
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Keywords: | marine drug equisetin host-acting compound autophagy |
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